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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434612Generated: October 29, 2026

2-(2-chloro-4-nitrophenoxy)naphthalene → 3-chloro-4-(2-naphthyloxy)aniline

https://huagongshe.com/reaction/434612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-chloro-4-nitrophenoxy)naphthaleneHCID 921588—
ReactantHCID 178418361HCID 178418361—
CatalystAdams' catalystHCID 345198—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
Product3-chloro-4-(2-naphthyloxy)anilineHCID 345128060.1%

Reaction Steps

3-Chloro-4-(2-naphthyloxy)nitrobenzene (14.8 g) and platinum dioxide (0.1 g) were suspended in a mixture of benzene and ethanol (1:1) (200 ml), and hydrogenation was carried out until 3.2 liters of hydrogen were absorbed. After removal of the solvent from the reaction mixture by distillation under reduced pressure, the residue was distilled in vacuo to give 3-chloro-4-(2-naphthyloxy)aniline (8 g) as a fraction boiling at 173° to 198° C./0.2 to 0.3 mmHg. M.P., 67°-69° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04399072
Source datasetuspto-grants-1983_08
ORD IDord-878d04351c52414c94f0f20873f9c511
Source noteuspto-grants-1983_08